US8236005B2 - System and method for preventing intraoperative fracture in cementless hip arthroplasty - Google Patents
System and method for preventing intraoperative fracture in cementless hip arthroplasty Download PDFInfo
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- US8236005B2 US8236005B2 US12/956,348 US95634810A US8236005B2 US 8236005 B2 US8236005 B2 US 8236005B2 US 95634810 A US95634810 A US 95634810A US 8236005 B2 US8236005 B2 US 8236005B2
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- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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- A61F2/4603—Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor for insertion or extraction of endoprosthetic joints or of accessories thereof
- A61F2/4607—Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor for insertion or extraction of endoprosthetic joints or of accessories thereof of hip femoral endoprostheses
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- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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Definitions
- the present invention relates generally to human joint replacement surgery, and particularly to a method and system that enable an orthopedic surgeon to monitor impaction data, such as vibration data, generated during impaction of the femoral component of a hip prosthesis into a femur and determine maximal femoral component interference fit and prosthetic stability to prevent femoral fractures during the impaction process.
- impaction data such as vibration data
- hip replacement is one of the most consistently successful surgical procedures in medicine.
- new minimally invasive surgical techniques in hip arthroplasty that offer numerous advantages over standard surgical approaches have been introduced. These purported advantages include shorter hospital stays, more rapid rehabilitation and recovery, less blood loss, and diminished postoperative pain.
- periprosthetic fractures associated with insertion of the femoral component. This is likely the result of diminished visibility, auditory and tactile feedback for the surgeon operating through smaller incisions.
- Intraoperative periprosthetic femur fractures may occur if the implant is impacted past the point of maximal interference fit, subjecting the cortical bone of the proximal femur to excessive hoop stresses.
- Such fractures especially if unrecognized, decrease the mechanical stability of the femoral component and may increase the risk of implant failure that is likely a result of diminished early bone ingrowth from fracture-induced instability and micromotion.
- the present invention provides a method and system for supplementing the surgeon's tactile and auditory senses by using damage identification techniques based on vibration characteristics associated with femoral component impaction to determine when a femoral component implant is fully seated.
- a method and system for monitoring impaction of a femoral component of a hip prosthesis into a femur in which impaction data generated during the impaction of the femoral component into the femur is received from at least one measurement transducer, such as a piezoelectric transducer (PZT) and/or an accelerometer, attached to the femoral component and is normalized by a data acquisition and analysis device.
- An impaction monitoring metric is calculated based on the normalized impaction data, and femoral component fit and stability data is then generated and output to a user interface based on the impaction monitoring metric.
- FIG. 1 is a schematic diagram of a system for monitoring femoral component fit and stability during impaction of a femoral component of a hip prosthesis into a femur according to an exemplary embodiment
- FIG. 2 is a flow diagram illustrating an exemplary method for monitoring impaction of a femoral component of a hip prosthesis into a femur;
- FIGS. 3A-3C are graphs of experimental data illustrating the relationship between percentage distance to final seated position of the femoral component and the percentage to total normalized metric within a seated interval based on data generated by the system shown in FIG. 1 ;
- FIG. 4 is a perspective view showing measurement transducers as attached to a femoral component of a hip prosthesis in accordance with yet another exemplary embodiment
- FIG. 5 is a perspective view showing in more detail the components in FIG. 4 as attached to the femoral component of the hip prosthesis;
- FIG. 6 is a table of additional signal processing techniques that may be applied to normalize femoral component impaction data for use in monitoring impaction of a femoral component of a hip prosthesis into a femur in accordance with various exemplary embodiments.
- FIG. 1 shows a system 100 for monitoring femoral component fit and stability during impaction of a tapered cementless femoral component 102 (femoral component) of a hip prosthesis into a femur 104 according to an exemplary embodiment.
- the femoral component 102 may be made, for example, from a titanium alloy with a porous titanium mesh around the circumference of the proximal half of the stem, such as a FiberMetal Taper component manufactured by Zimmer, Inc. of Warsaw, Ind.
- the system 100 is designed for use in minimally invasive cementless hip arthroplasty in which the surgeon must determine proper seating of the femoral component 102 with minimal tactile and auditory feedback to avoid intraoperative fractures in the femur caused by overseating of the femoral component.
- the system 100 is also generally applicable to any joint replacement procedure that involves impaction of a prosthetic component into bone and that requires accurate component seating.
- the system 100 includes a testing component 106 on which is mounted at least one measurement transducer, such as accelerometers 108 , 110 and 112 , a data acquisition and analysis device 114 in communication with the measurement transducers 108 , 110 , 112 , and a user interface 116 in communication with the data acquisition and analysis device 114 .
- a measurement transducer such as accelerometers 108 , 110 and 112
- a data acquisition and analysis device 114 in communication with the measurement transducers 108 , 110 , 112
- a user interface 116 in communication with the data acquisition and analysis device 114 .
- the testing component 106 is preferably a reusable component, such as a 6061 aluminum fixture that may be bolted or otherwise attached to the femoral component 102 .
- the term testing component as used throughout the present description refers generally to the component or components used to generate femoral component impaction data.
- the testing component 106 is configured to function essentially as a mounting block for the accelerometers 108 , 110 , 112 .
- Each of the accelerometers 108 , 110 , 112 is operable to detect vibrations resulting from the impaction of the femoral component 102 into the femur 104 and to correspondingly generate detection signals including impaction data.
- the accelerometer 108 is oriented in an impaction direction of the femoral component along a relative z axis, while the transverse accelerometers 110 , 112 are oriented orthogonally to the relative z axis along relative x and y axes, respectively.
- the accelerometer 108 oriented along the z axis is preferably a shock accelerometer, such as a PCB Piezotronics Model No. 352B01 accelerometer, with a nominal sensitivity of approximately 1 mV/g, a measurement range of approximately 10,000 g and a frequency range of approximately 20 kHz.
- the accelerometers 110 , 112 respectively oriented along the x and y axes are each preferably an accelerometer, such as a PCB Piezotronics Model No. 353B13 accelerometer, with a nominal sensitivity of approximately 5 mV/g, a measurement range of approximately 2,000 g and a frequency range of approximately 20 kHz.
- an accelerometer such as a PCB Piezotronics Model No. 353B13 accelerometer, with a nominal sensitivity of approximately 5 mV/g, a measurement range of approximately 2,000 g and a frequency range of approximately 20 kHz.
- the accelerometer 108 is configured to detect the impaction force generated when a hammer, such as the hammer 118 , impacts a punch 120 .
- the hammer 118 may be a standard surgeon's hammer or may be instrumented with a force transducer. If implemented with a force transducer, such as Piezotronics Model No. PCB 086C05, with a sensitivity of approximately 1 mV/lbf, a frequency range of approximately 5 kHz and an amplitude range of 5,000 lbf, the hammer 118 is placed in communication with the data acquisition and analysis device 114 as shown in FIG. 1 to enable the data acquisition and analysis device 114 to record input force generated by the hammer 118 .
- a force transducer such as Piezotronics Model No. PCB 086C05
- the hammer 118 may also be fitted with a hard tip 118 a to better simulate a standard surgeon's hammer.
- the punch 120 may include a bottom end 120 a that fits into a slot in the top end 102 a of the femoral component 102 .
- the punch 120 may or may not be placed in communication with the data acquisition and analysis device 114 depending upon the particular system set-up.
- the data acquisition and analysis device 114 is configured to receive the impaction data from the accelerometers 108 , 110 , 112 , the hammer 118 and/or the punch 120 , normalize the impaction data into a usable format as normalized impaction data, calculate an impaction monitoring metric and output femoral component fit and stability data based on the impaction monitoring metric.
- the data acquisition and analysis device 114 is shown as including a signal analyzer 122 , such as an eight channel Dactron Spectrabook Dynamic Signal Analyzer, manufactured by LDS Test and Measurement, LLC, and a laptop computer 124 that runs data acquisition software such as RT Pro software.
- the computer 124 also executes instructions stored on a computer readable medium, such as a hard drive or CD-ROM, with the instructions including a computer implemented method for monitoring impaction of a femoral component of a hip prosthesis into a femur, such as the method that will be discussed below in connection with the flow diagram 200 in FIG. 2 .
- a computer readable medium such as a hard drive or CD-ROM
- the user interface 116 is configured to receive the femoral component fit and stability data output from the data acquisition and analysis device and provide feedback indicative of the femoral component fit and stability data to the surgeon.
- the user interface 116 may be a computer display or any other visual, audio or audiovisual device capable of providing to the surgeon feedback that is indicative of the femoral component fit and stability data and that is generated in a manner that will now be discussed.
- the data acquisition and analysis device 114 receives impaction data generated during the impaction of the femoral component 102 into the femur 104 from at least one of the accelerometers 108 , 110 , 112 attached to the femoral component 102 by way of the testing component 106 .
- the z-axis acceleration most closely corresponds to the seating of the femoral component. Therefore, use of the data from the accelerometer 108 will be assumed for purposes of the present description.
- the data acquisition and analysis device 114 when the data acquisition and analysis device 114 receives the impaction data, such as impact force data from the accelerometer 108 and acceleration data from the accelerometers 110 , 112 , the data acquisition and analysis device 114 normalizes the impaction data into a usable format as normalized impaction data. According to the presently discussed exemplary embodiment, impaction data is normalized to remove the effect of the magnitude of the input signal.
- the data acquisition and analysis device 114 calculates an impaction monitoring metric indicative of the time that it takes a measured impaction signal to obtain a fraction, or percentage, of its total norm. This metric is associated with an increase in signal damping that occurs as the femoral component 102 nears a fully seated position in the femur 104 . Such a technique is advantageous in that input data from the hammer 118 and/or the punch 120 is not required.
- the data acquisition and analysis device 114 is programmed to calculate a total norm of an acceleration signal including the impaction data as shown in Eq. 1:
- N is a number of points in a time interval to be analyzed
- a is an acceleration measurement taken at an i th point by the accelerometer 108 .
- the data acquisition and analysis device 114 first filters any linear trends associated with the acceleration data prior to calculating E j using Eq. 2.
- the data acquisition and analysis device 114 then outputs femoral component fit and stability data based on the calculated impaction monitoring metric to the user interface 116 to enable the surgeon to determine whether the femoral component 102 is fully seated.
- the data acquisition and analysis device 114 monitors for a subsequent impaction hit. If no such hit is detected, the method ends. If another impaction hit is detected, the method returns to 202 and is repeated.
- FIGS. 3A , 3 B and 3 C graphically illustrate experimental femoral component impaction results for three separate cementless hip arthroplasty procedures as expressed by percent distance to final seated position versus number of impaction hits.
- the shaded area represents a range of hits in which the femoral component is considered to be seated, factoring in the somewhat subjective nature of when different surgeons would consider the femoral component to be seated.
- the dotted lines in each graph represent the actual percentage of distance of the femoral component to its final seated position as measured from the top of the prosthesis to the opening of the femoral canal, while the solid lines in each graph represent the percentage of the total norm of an impaction signal as calculated in Eq. 2 above.
- calculation of the 99% to norm metric represents an accurate method of determining when the femoral component is seated.
- the above data was generated under the following experimental conditions. Cadaveric specimens were used, with each one being placed in the lateral decubitus position. A standard anterolateral approach to the hip was utilized to expose and dislocate the hip, as it occurs during total hip arthroplasty. Dislocation was performed after an anterior capsulotomy and was achieved with hip flexion, adduction and external rotation. The operative leg was then positioned over the contralateral extremity to adequately expose the proximal femur. Radiographic evaluation was unavailable prior to the procedure. Therefore, the femoral neck osteotomy and femoral preparation were performed without the benefit of preoperatively assessing the femoral size, canal shape, anatomy identification, and overall bone quality.
- the femoral neck osteotomy was made approximately one finger-width above the lesser trochanter, which was visualized directly.
- the removed femoral neck was sent to a laboratory for further analysis of bone quality including bone mineral density (BMD).
- BMD bone mineral density
- a box osteotome was used to enter the proximal femur and ensure adequate removal of the lateral femoral neck.
- the T-handled Charnley awl was then used by hand to establish intramedullary access and alignment. Reamers were not used during any portion of the femoral preparation.
- Broaching of the femur was then performed utilizing broaches of increasing sizes until appropriate axial and rotational stability was obtained as determined by the performing surgeon.
- the broaches were always inserted in an orientation that approximated the femoral neck anteversion. Once the final broach was determined, the identical sized femoral implant was selected.
- the femoral component is shown at 102 .
- one or more impaction measurement transducers such as a z-axis accelerometer 408 oriented along an impaction direction on a relative z axis and a piezoelectric transducer (PZT) patch 430 , are directly attached to the femoral component 102 rather than to an instrumented testing component, while transverse accelerometers 110 , 112 are mounted on, for example, a block 414 that is attached to the femoral component 102 .
- PZT piezoelectric transducer
- the z-axis accelerometer 408 and the PZT patch 430 may be considered the testing component if utilized without the transverse accelerometers 110 , 112 .
- the PZT patch 430 may be, for example, a 0.25 inch diameter model APC 850 patch attached by, for example, an adhesive resin cement such as M-Bond.
- a femoral component impedance measurement may be taken through the PZT patch 430 , which is in communication with the data acquisition and analysis device 116 of FIG. 1 , and frequency response functions (FRFs) between the PZT patch 430 and the accelerometers 408 , 110 , 112 may be determined using the data acquisition and analysis device 116 .
- FRFs frequency response functions
- a band-limited Gaussian white excitation may then be input through the PZT patch 430 between hits, sampled at a rate of, for example, 200 kHz and the FRFs then averaged a predetermined number of times to eliminate noise.
- a Hanning window may be applied to the data to minimize leakage.
- the impedance and FRF measurements may be repeated and used as baselines for subsequent measurements.
- acceleration time history data may be acquired from the accelerometers 408 , 110 , 112 and the force transducer on the hammer 118 may be used to acquire the force input.
- a predetermined number of data samples may be taken without a window at a sampling rate of, for example, 40 kHz.
- the data acquisition is triggered using the force input to obtain 10 pre-data points. Therefore, as the force crosses a predetermined threshold, the data acquisition and analysis device 114 may acquire force signals as well as 10 samples prior to impaction, thereby enabling signals to be acquired in their entirety.
- the data acquisition and analysis device 114 may be programmed with software to calculate representative FRFs from one of the accelerometers 408 , 110 , 112 based on the excitation signals generated by the PZT patch 430 . It has been noted through experimentation that an impaction monitoring metric calculated between impaction hits based on convergence of resonance signal frequencies and anti-resonance signal frequencies in the 10.5 kHz-12 kHz band or based on peak magnitudes of these frequencies in the 9 kHz-11 kHz band are indicative of whether a femoral component is or is not fully seated.
- FIG. 6 is a table of additional processing techniques capable of being used in systems similar to those described above to calculate impaction monitoring metrics.
- Each of the listed processing techniques may be implemented by programming the above discussed data acquisition and analysis device 114 in a manner that will be understood by one skilled in the art to generate metrics indicative of femoral component seating based on signals received from one or more measurement transducers such as the accelerometers 108 , 110 , 112 the hammer 118 and/or the punch 120 in FIG. 1 and/or the accelerometer 408 and the PZT patch 430 in FIG. 4 .
- the measurement transducer signals may be processed to produce metrics based on signal frequency, signal time history, signal stationarity, signal interrelation, neural network calculations and/or signals indicative of energy dissipation.
Abstract
Description
where N is a number of points in a time interval to be analyzed and a is an acceleration measurement taken at an ith point by the
where a time t(j) corresponding to a fractional value Ej within a predetermined range indicative of the femoral component being fully seated is determined for each of a plurality of femoral component impaction hits. Based on experimental evidence, it has been determined that a time tj corresponding to a value Ej=0.99 provides an accurate indication of when the
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US11/604,873 US7879043B2 (en) | 2006-11-28 | 2006-11-28 | System and method for preventing intraoperative fracture in cementless hip arthroplasty |
US12/956,348 US8236005B2 (en) | 2006-11-28 | 2010-11-30 | System and method for preventing intraoperative fracture in cementless hip arthroplasty |
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US8709092B2 (en) | 2011-02-16 | 2014-04-29 | Genesis Medical Devices, LLC | Periprosthetic fracture management enhancements |
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US11364361B2 (en) | 2018-04-20 | 2022-06-21 | Neuroenhancement Lab, LLC | System and method for inducing sleep by transplanting mental states |
US11426243B2 (en) | 2020-02-12 | 2022-08-30 | DePuy Synthes Products, Inc. | Technologies for monitoring and predicting impaction state of an orthopaedic surgical implement during an orthopaedic surgical procedure |
US11452839B2 (en) | 2018-09-14 | 2022-09-27 | Neuroenhancement Lab, LLC | System and method of improving sleep |
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